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SIGLEC1 protein levels

HSPA12B · rs143974404

Where this position leads

Condition: Celiac Disease

rs143974404 Condition: Celiac Disease Celiac Disease Condition rs143974404 rs143974404 HSPA12B

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.473 higher (95% confidence interval 0.33-0.62); p = 3 × 10−12.

How common The T allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 20, band 20p13 — a synonymous change in HSPA12B.

What each result means

C/C No copy of the version the research linked to SIGLEC1 protein levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to SIGLEC1 protein levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to SIGLEC1 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs143974404

What is rs143974404?

rs143974404 is a single position in the genome, in or near the HSPA12B gene. Published research associates it with siglec1 protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs143974404 linked to?

On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs143974404 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs143974404 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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SIGLEC1 protein levels (rs143974404). MyGeneLog™. https://www.mygenelog.com/variants/rs143974404

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